Title of Invention

"ESTERIFICATION CATALYST AND PROCESS FOR THE ESTERIFICATION OF ACIDS IN A HYDROCARBONS CONTAINING FEED"

Abstract The present invention relates to an esterification process for the reduction of acids in a hydrocarbon containing composition, said process including contacting the hydrocarbon with an esterification catalyst at esterification temperature and pressure. The esterification catalyst include metal oxides which include one or more oxides selected from the molybdenum oxide, tungsten oxide and transition metal oxides in group 1b to VIIIb.
Full Text ESTERIFICATION CATALYST AND PROCESS FOR THE ESTERIFICATION
OF ACIDS IN A HYDROCARBONS CONTAINING FEED
Field of the invention
The invention provides an esterifieation catalyst and an esterification process for
the esterification of acids in a hydrocarbons containing feed stream,
Background to the Invention
Fischer-Tropsch (FT) product streams are known to contain organic acids,
carbonyls, alcohols and other oxygenates, but no sulphur compounds. Removing
acids from FT products would allow these products to be hydrogenated at lower
temperatures over nickel or other catalyst without introducing sulphur to the
process. Removal of acids upstream of the refinery would also reduce the
problem of corrosion which is exacerbated by the presence of water in the
hydrocarbon streams.
Summary of the Invention
According to a first aspect of the invention, there is provided an esterification
catalyst including one or more catalytically active metal oxides.
The metal oxides may include one or more oxides selected from transition metal
oxides in group Ib to Vlllb, for example molybdenum oxide or tungsten oxide.
The molybdenum, the tungsten, or the transition metal oxide of the catalyst may
be supported on a substrate.
The substrate may be alumina, silica-alumina, silica or any other suitable
substrate.
According to a second aspect of the invention there is provided an esterification
process for the reduction of acids in a hydrocarbon containing composition, said
process including contacting the hydrocarbon containing composition with an
esterification catalyst at esterfication temperature and pressure.
The esterification catalyst may be a catalyst substantially as described above.
The esterification catalyst may be a catalyst selected from the group of transition
metal oxides in group Ib to VIHb on alumina substrate, including molybdenum
oxide on alumina catalyst and tungsten oxide on alumina catalyst.
The esterification temperature may be from 100°C to 320°C.
The esterification temperature may be from 170°C to 25O°C,
Typically the esterification temperature is from 190°C to 210°C.
The esterification pressure may be from atmospheric pressure to 100 Bar,
typically from 1 to 55 Bar,
The hydrocarbon containing composition may include hydrocarbons of less than
24 carbons i.e. lower than C24.
The hydrocarbon containing composition may be a C4 to C2o hydrocarbons
containing composition.
The hydrocarbon containing composition may be a Fischer-Tropsch (FT)
condensate fraction.
By FT eondensate fraction is meant a eondensate fraction of the Fischer-Tropsch
reaction products, The eondensate fraction is typically obtained as the light
stream or overhead stream from a separator after a Fischer-Tropsch reactor in
which the Fischer-Tropsch reaction has taken place. Table A below provides
(Table Removed)
typical data for the FT eondensate stream.
The hydrocarbon eondensate fraction may be a distilled fraction from the FT
eondensate fraction. An example of such distilled fraction is shown in table B.
(Table Removed)
The hydrocarbon containing composition may have an acid level of 0.5 mg
KOH/g or higher.
Typically, the acid level in the hydrocarbon containing composition may be as
high as 12 mg KOH/g.
The alcohol to acid ratio in the FT hydrocarbon may be between 9 and 92 on a
molar basis.
Methanol or another alcohol may be added to the FT hydrocarbon feed to
increase the alcohol to acid ratio.
The product of the process may have an acid level of less than or equal to 0.5
mg KOH/g, generally from 0.1 mg KOH/g to 0.3 mg KOH/g.
The process may be carried out in a continuous flow reactor, like a trickle bed or
a flooded bed reactor. The process may also be carried out in a batch reactor.
The process may be carried out at an LHSV of from 0.1 to 5 h"1.
The process may be carried out at an LHSV of from 0.5 and 2 h'1.
Examples of Performing the Invention
The examples that follow are not intended to limit the scope of the invention and
are by way of illustration of the invention only.
Catalysts and operating procedures
A commercial molybdenum on alumina catalyst from BASF (M8-30) was used for
experiments 1 to 5. The catalyst is produced in 5 mm diameter extrudates. The
extrudates were crushed and sieved between 0,5 and 2,83 mm and diluted 1:1
with carborundum (0,5-2mm).
(Table Removed)
The catalyst was dried in situ in a hydrogen flow at 125°C and pretreated with
hydrogen either at 470°C for 10 hours or at 250°C for 5 hours or heated to
operating temperature. The temperature programmed reduction (TPR) shows a
reaction with hydrogen around 430°C.
In experiment 6 an extruded WOa/AfeOa catalyst containing about 20 % tungsten
oxide was used which was ground to a particle size between 0.5 and 1 mm.
The experiments 1 to 4 were carried in a 27,5 mm ID bench scale reactor with a
total length of 1,5 meter. Bed temperatures were measured with 6 thermocouples
axially spaced inside a 6mm OD thermocouple sheath. The reactor was operated
in the down flow mode, at 55 bar, 0.56 to 1.5 l/(lcat.h) liquid hourly space velocity
(LHSV) and between 385 and 500 ln/(lcat.h) hydrogen GHSV.
Experiments 5 and 6 were carried out in microreactor with an internal diameter of
12 mm. Bed temperatures were measured with 2 thermocouples axially spaced
inside a 3 mm OD thermocouple sheath. The reactor was operated in the down
flow mode at 5 bar and 0.56 to 0.67 l/(lcat.h) liquid hourly space velocity (LHSV)
and between 300 and 450 ln/(lcat.h) hydrogen GHSV.
Examples
Example 1
The feed in the first experiment consisted of a C4-C20 Fischer-Tropsch product
cut. The hydrocarbon product was passed through a caustic wash which reduced
the acids to about 0,5 mg KOH/g. The molar ratio of alcohols to acids in the
hydrocarbon feed was 92,
The catalyst was pretreated in hydrogen at 470°C.
The results are shown in table 3 below
(Table Removed)
Fresh MoOx/AI2O3 catalyst showed initially considerable catalytic activity towards
both esterification and dehydrogenation/dehydration reactions. At the beginning
of the run all oxygenates were removed at 250*C and the olefins concentration
doubled from 40 to 80 gBr/100g. The latter reactions were however short lived.
The residual acids in the effluent stream was 0,01 mg KOH/g.
In the same experiment, in the temperature range of 190 to 210"C, the acids still
reacted nearly completely to esters but less of the other oxygenates reacted and
over time side reactions decreased.
At the lower temperatue the olefinity of the effluent was similar to the value of the
feed.
Example 2
In this example the feed consisted of C4 to C20 paraffin with a higher acid level
(2,3 mg KOH/g). The alcohol concentration was the same as in the previous
feed, about 7 mass% as €7 alcohol. The molar ratio of alcohol to acid of this feed
was 16,5.
The catalyst treatment was the same as in example 1.
The results are shown in table 3 above.
The residual acids in the effluent were between 0,02 and 0,03 mgKOH/g at
210°C. When the temperature was increased to 250°C (after about 5 days), the
residual acid level increased to 0.15 mg KOH/g. This may be ascribed to a
decrease of the alcohol concentration due to secondary reactions. As a result the
alcohol to acid ratio decreased causing a decrease in the conversion to esters.
After 3 weeks on line the oxygenates could no longer be removed at a
temperature of 250"C. The temperature had to be increased to 310°C before the
bulk of the oxygenates was removed.
Example 3
in this experiment the molybdenum oxide on alumina catalyst was pretreated in
hydrogen at 250°C.
The feed for this experiment was a light cpndensate fraction derived from lowtemperature
Fischer-Tropsch synthesis (mainly in the naphtha and diesel range
with a small fraction waxy material suspended in it). The acids varied between
1,9and2,5mgKOH/g.
The results are shown in table 4 below
At a temperature of 210°C, 1 h'1 IHSV and an alcohol to acid ratio of 14 the
conversion of the acids .was 98.8 % resulting in an acid number of 0.03 mg
KOH/g in the effluent. The same results were obtained at 1,5 h~1 LHSV, which
indicated that the reaction was close to equilibrium.
The stability of the catalyst was tested at 220°C for 13 days at 1 rf1 LHSV with a
different feed (alcohol to acid ratio of 19). The residual acids were 0.05 mgKOH/g
and remained stable for as long as these conditions were maintained.
At temperatures between 250 and 290°C the acid content of the product
increased and only at 310°C did they decrease. Significantly, the olefinity of the
product did not increase at these temperatures.
(Table Removed)
Carbonyls were only partly removed and the temperature made little difference to
the conversion.
Depending on the temperature, alcohols and carbonyls may react to form a
range of compounds and a change in the alcohol to acid ratio will shift the
equilibrium from ester to free acids.
Apart from esterification, alcohols can undergo a variety of other reactions:
• aldol condensation with aldehydes
• acetal and ether formation
• dehydration to olefins
There was insufficient evidence to conclude that alcohols were dehydrated to
olefins because the olefin level did not increase consistently. Temperatures of
well above 300°C are required to dehydrate significant amounts of ethanol and
propanol to the corresponding olefins.
Example 4
The feed in this experiment consisted of a C10-C13 Fischer Tropsch product cut.
The hydrocarbon product was high in acids (about 12,5 mg KOH/g) and
contained other oxygenates. Methanol was co-fed with the Frscher-Tropsch
product at such ratio that the molar ratio of alcohols to acids in the hydrocarbon
feed was equal to 10.
The catalyst was molybdenum oxide on alumina which was pretreated in
hydrogen at 250°C.
The results are shown in table 5 below.
(Table Removed)
Example 5
The catalyst was the same as used in experiment 1, but the reaction was carried
out in a microreactor. 20 ml Catalyst with a particle size between 0,5 and 1,0 mm
was loaded. The catalyst was heated up in a hydrogen stream to the reaction
temperature at which point the feed was introduced. The feed consisted of a C13-
C14 FT hydrocarbon product fraction with an acid number of 12,6 mg KOH/g.
Methanol was co-fed with the FT hydrocarbon. The ratio of alcohol to acid in the
mixture was between 9 and 12 on a molar basis. The reaction was carried out at
0,67 h"1 LHSV (hydrocarbon feed), 190 h'1 hydrogen GHSV and 5 bar g pressure.
A reduction of the acids in the hydrocarbon from 12,6 to 0,3 mg KOH/g was
achieved in the temperature range of 210 to 230 °C. This amounts to a
conversion of 97,7 % of the acids to esters in a single pass.
Example 6
The catalyst in this example was tungsten oxide on alumina, containing about 20
mass % W03.
The equipment and the experimental conditions were the same as described in
example 5.
Similar to the previous example, the catalyst was heated up in a hydrogen
stream to reaction temperature and the feed introduced.
The results are shown in table 6. The acid concentration in the hydrocarbon was
reduced to 0,3 mg KOH/g at 5 bar g, 210 °C, 0,71 IT1 LHSV and an alcohol/acic
ration of 17.
(Table Removed)



ESTERIFICATION CATALYST AND PROCESS FOR THE ESTERIFICATION
OF ACIDS IN A HYDROCARBONS CONTAINING FEED
Field of the invention
The invention provides an esterifieation catalyst and an esterification process for
the esterification of acids in a hydrocarbons containing feed stream,
Background to the Invention
Fischer-Tropsch (FT) product streams are known to contain organic acids,
carbonyls, alcohols and other oxygenates, but no sulphur compounds. Removing
acids from FT products would allow these products to be hydrogenated at lower
temperatures over nickel or other catalyst without introducing sulphur to the
process. Removal of acids upstream of the refinery would also reduce the
problem of corrosion which is exacerbated by the presence of water in the
hydrocarbon streams.
Summary of the Invention
According to a first aspect of the invention, there is provided an esterification
catalyst including one or more catalytically active metal oxides.
The metal oxides may include one or more oxides selected from transition metal
oxides in group Ib to Vlllb, for example molybdenum oxide or tungsten oxide.
The molybdenum, the tungsten, or the transition metal oxide of the catalyst may
be supported on a substrate.
The substrate may be alumina, silica-alumina, silica or any other suitable
substrate.
According to a second aspect of the invention there is provided an esterification
process for the reduction of acids in a hydrocarbon containing composition, said
process including contacting the hydrocarbon containing composition with an
esterification catalyst at esterfication temperature and pressure.
The esterification catalyst may be a catalyst substantially as described above.
The esterification catalyst may be a catalyst selected from the group of transition
metal oxides in group Ib to VIHb on alumina substrate, including molybdenum
oxide on alumina catalyst and tungsten oxide on alumina catalyst.
The esterification temperature may be from 100°C to 320°C.
The esterification temperature may be from 170°C to 250°C,
Typically the esterification temperature is from 190°C to 210°C.
The esterification pressure may be from atmospheric pressure to 100 Bar,
typically from 1 to 55 Bar,
The hydrocarbon containing composition may include hydrocarbons of less than
24 carbons i.e. lower than C34.
The hydrocarbon containing composition may be a C4 to C20 hydrocarbons
containing composition.
The hydrocarbon containing composition may be a Fischer-Tropsch (FT)
condensate fraction.
By FT eondensate fraction is meant a eondensate fraction of the Fischer-Tropsch
reaction products, The eondensate fraction is typically obtained as the light
stream or overhead stream from a separator after a Fischer-Tropsch reactor in
which the Fischer-Tropsch reaction has taken place. Table A below provides
typical data for the FT eondensate stream.
(Table Removed)
The hydrocarbon eondensate fraction may be a distilled fraction from the FT
eondensate fraction. An example of such distilled fraction is shown in table B.
(Table Removed)
The hydrocarbon containing composition may have an acid level of 0.5 mg
KOH/g or higher.
Typically, the acid level in the hydrocarbon containing composition may be as
high as 12 mg KOH/g.
The alcohol to acid ratio in the FT hydrocarbon may be between 9 and 92 on a
molar basis.
Methanol or another alcohol may be added to the FT hydrocarbon feed to
increase the alcohol to acid ratio.
The product of the process may have an acid level of less than or equal to 0.5
mg KOH/g, generally from 0.1 mg KOH/g to 0.3 mg KOH/g.
The process may be carried out in a continuous flow reactor, like a trickle bed or
a flooded bed reactor. The process may also be carried out in a batch reactor.
The process may be carried out at an LHSV of from 0.1 to 5 h"1.
The process may be carried out at an LHSV of from 0.5 and 2 h'1.
Examples of Performing the Invention
The examples that follow are not intended to limit the scope of the invention and
are by way of illustration of the invention only.
Catalysts and operating procedures
A commercial molybdenum on alumina catalyst from BASF (M8-30) was used for
experiments 1 to 5. The catalyst is produced in 5 mm diameter extrudates. The
extrudates were crushed and sieved between 0,5 and 2,83 mm and diluted 1:1
with carborundum (0,5-2mm).
(Table Removed)
The catalyst was dried in situ in a hydrogen flow at 125°C and pretreated with
hydrogen either at 470°C for 10 hours or at 250°C for 5 hours or heated to
operating temperature. The temperature programmed reduction (TPR) shows a
reaction with hydrogen around 430°C.
In experiment 6 an extruded WOa/AfeOa catalyst containing about 20 % tungsten
oxide was used which was ground to a particle size between 0.5 and 1 mm.
The experiments 1 to 4 were carried in a 27,5 mm ID bench scale reactor with a
total length of 1,5 meter. Bed temperatures were measured with 6 thermocouples
axially spaced inside a 6mm OD thermocouple sheath. The reactor was operated
in the down flow mode, at 55 bar, 0.56 to 1.5 l/(lcat.h) liquid hourly space velocity
(LHSV) and between 385 and 500 ln/(lcat.h) hydrogen GHSV.
Experiments 5 and 6 were carried out in microreactor with an internal diameter of
12 mm. Bed temperatures were measured with 2 thermocouples axially spaced
inside a 3 mm OD thermocouple sheath. The reactor was operated in the down
flow mode at 5 bar and 0.56 to 0.67 l/(lcat.h) liquid hourly space velocity (LHSV)
and between 300 and 450 ln/(lcat.h) hydrogen GHSV.
Examples
Example 1
The feed in the first experiment consisted of a C4-C20 Fischer-Tropsch product
cut. The hydrocarbon product was passed through a caustic wash which reduced
the acids to about 0,5 mg KOH/g. The molar ratio of alcohols to acids in the
hydrocarbon feed was 92,
The catalyst was pretreated in hydrogen at 470°C.
The results are shown in table 3 below
(Table Removed)
Fresh MoOx/AI2O3 catalyst showed initially considerable catalytic activity towards
both esterification and dehydrogenation/dehydration reactions. At the beginning
of the run all oxygenates were removed at 250*C and the olefins concentration
doubled from 40 to 80 gBr/100g. The latter reactions were however short lived.
The residual acids in the effluent stream was 0,01 mg KOH/g.
In the same experiment, in the temperature range of 190 to 210"C, the acids still
reacted nearly completely to esters but less of the other oxygenates reacted and
over time side reactions decreased.
At the lower temperatue the olefinity of the effluent was similar to the value of the
feed.
Example 2
In this example the feed consisted of C4 to C2o paraffin with a higher acid level
(2,3 mg KOH/g). The alcohol concentration was the same as in the previous
feed, about 7 mass% as €7 alcohol. The molar ratio of alcohol to acid of this feed
was 16,5.
The catalyst treatment was the same as in example 1.
The results are shown in table 3 above.
The residual acids in the effluent were between 0,02 and 0,03 mgKOH/g at
210°C. When the temperature was increased to 250°C (after about 5 days), the
residual acid level increased to 0.15 mg KOH/g. This may be ascribed to a
decrease of the alcohol concentration due to secondary reactions. As a result the
alcohol to acid ratio decreased causing a decrease in the conversion to esters.
After 3 weeks on line the oxygenates could no longer be removed at a
temperature of 250"C. The temperature had to be increased to 310°C before the
bulk of the oxygenates was removed.
Example 3
in this experiment the molybdenum oxide on alumina catalyst was pretreated in
hydrogen at 250°C.
The feed for this experiment was a light cpndensate fraction derived from lowtemperature
Fischer-Tropsch synthesis (mainly in the naphtha and diesel range
with a small fraction waxy material suspended in it). The acids varied between
1,9and2,5mgKOH/g.
The results are shown in table 4 below
At a temperature of 210°C, 1 h'1 IHSV and an alcohol to acid ratio of 14 the
conversion of the acids .was 98.8 % resulting in an acid number of 0.03 mg
KOH/g in the effluent. The same results were obtained at 1,5 h~1 LHSV, which
indicated that the reaction was close to equilibrium.
The stability of the catalyst was tested at 220°C for 13 days at 1 rf1 LHSV with a
different feed (alcohol to acid ratio of 19). The residual acids were 0.05 mgKOH/g
and remained stable for as long as these conditions were maintained.
At temperatures between 250 and 290°C the acid content of the product
increased and only at 310°C did they decrease. Significantly, the olefinity of the
product did not increase at these temperatures.
(Table Removed)
Carbonyls were only partly removed and the temperature made little difference to
the conversion.
Depending on the temperature, alcohols and carbonyls may react to form a
range of compounds and a change in the alcohol to acid ratio will shift the
equilibrium from ester to free acids.
Apart from esterification, alcohols can undergo a variety of other reactions:
• aldol condensation with aldehydes
• acetal and ether formation
• dehydration to olefins
There was insufficient evidence to conclude that alcohols were dehydrated to
olefins because the olefin level did not increase consistently. Temperatures of
well above 300°C are required to dehydrate significant amounts of ethanol and
propanol to the corresponding olefins.
Example 4
The feed in this experiment consisted of a C10-C13 Fischer Tropsch product cut.
The hydrocarbon product was high in acids (about 12,5 mg KOH/g) and
contained other oxygenates. Methanol was co-fed with the Frscher-Tropsch
product at such ratio that the molar ratio of alcohols to acids in the hydrocarbon
feed was equal to 10.
The catalyst was molybdenum oxide on alumina which was pretreated in
hydrogen at 250°C.
The results are shown in table 5 below.
(Table Removed)
Example 5
The catalyst was the same as used in experiment 1, but the reaction was carried
out in a microreactor. 20 ml Catalyst with a particle size between 0,5 and 1,0 mm
was loaded. The catalyst was heated up in a hydrogen stream to the reaction
temperature at which point the feed was introduced. The feed consisted of a C13-
CM FT hydrocarbon product fraction with an acid number of 12,6 mg KOH/g.
Methanol was co-fed with the FT hydrocarbon. The ratio of alcohol to acid in the
mixture was between 9 and 12 on a molar basis. The reaction was carried out at
0,67 h"1 LHSV (hydrocarbon feed), 190 h'1 hydrogen GHSV and 5 bar g pressure.
A reduction of the acids in the hydrocarbon from 12,6 to 0,3 mg KOH/g was
achieved in the temperature range of 210 to 230 °C. This amounts to a
conversion of 97,7 % of the acids to esters in a single pass.
Example 6
The catalyst in this example was tungsten oxide on alumina, containing about 20
mass % W03.
The equipment and the experimental conditions were the same as described in
example 5.
Similar to the previous example, the catalyst was heated up in a hydrogen
stream to reaction temperature and the feed introduced.
The results are shown in table 6. The acid concentration in the hydrocarbon was
reduced to 0,3 mg KOH/g at 5 bar g, 210 °C, 0,71 IT1 LHSV and an alcohol/acic
ration of 17.
(Table Removed)






WE CLAIM
1. An esteriflcation process for the reduction of acids in a hydrocarbon containing
composition, said process including contacting the hydrocarbon containing
composition having C4 to C20 hydrocarbon and /or Fischer-Tropsch condensate
fraction, with an esteriflcation catalyst at esteriflcation temperature in the range of
100°C to 320°C and pressure in the range of atmospheric pressure to 100 bar.
2. An esteriflcation process as claimed in claim 1, wherein the esteriflcation catalyst
includes one or more catalytically active metal oxides.
3. An esterification process as claimed in claim 2, wherein the metal oxides include
one or more oxides selected from transition metals in group Ib to VIIIb.
4. An esterification process as claimed in claim 2, wherein the metal oxide consists
of molybdenum oxide or tungsten oxide.
5. An esterification process as claimed in claims 2 to 4, wherein the molybdenum,
the tungsten, or any other transition metal oxide is supported on a substrate.
6. An esterification process as claimed in claim 5, wherein the substrate is alumina,
silica & alumina, or silica.
7. An esterification process as claimed in any one of claims 1 to 6, wherein the
esterification catalyst is a catalyst selected from the group of transition metal
oxides in group Ib to VIIIb on alumina catalyst, including molybdenum oxide on
alumina catalyst and tungsten oxide on alumina catalyst.
8. An esterification process as claimed in any one of the preceding claims, wherein
the esteriflcation temperature is in the range of 170°C to 250°C, more typically
froml90°C to210°C.
9. An esterification process as claimed in any one of the preceding claims 1 to 8,
wherein the esterification pressure is in the range of atmospheric pressure to 100
Bar, typically from 1 to 55 bar.
10. An esterification process as claimed in claim 11, wherein the hydrocarbon
condensate fraction is a distilled fraction from the FT condensate fraction.
11. An esterification process as claimed in any one of the preceding claims 1 to 10,
wherein the hydrocarbon containing composition has an acid level of 0.5 mg
KOH/g or higher, typically up to 12 mg KQH/g.
12. An esterification process as claimed in any one of claims 1 to 11, wherein the
alcohol to acid ratio in the FT hydrocarbon is between 9 and 92 on a molar basis.
13. An esterification process as claimed in any one of claims 1 to 12, wherein
methanol or another alcohol is added to the FT hydrocarbon feed to increase the
alcohol to acid ratio.
14. An esterification process as claimed in any one of the preceding claims 1 to 13,
wherein the product of the process has an acid level of less than or equal to 0.5
mg KQH/g, typically from 0.1 mg KOH/g to 0.3 mg KOH/g.
15. An esterification process as claimed in claims 1 to 14, wherein the process is
carried out in a continuous flow reactor.
16. An esterification process as claimed in claims 1 to 15, wherein the process is
carried out at an LHSV of from 0.1 to 5h-1.

Documents:

3356-delnp-2005-abstract.pdf

3356-delnp-2005-claims.pdf

3356-DELNP-2005-Correspondence-Others-(16-04-2010).pdf

3356-delnp-2005-correspondence-others.pdf

3356-delnp-2005-description (complete).pdf

3356-delnp-2005-form-1.pdf

3356-delnp-2005-form-13.pdf

3356-delnp-2005-form-18.pdf

3356-delnp-2005-form-2.pdf

3356-delnp-2005-form-26.pdf

3356-delnp-2005-form-3.pdf

3356-delnp-2005-form-5.pdf

3356-delnp-2005-pct-237.pdf

3356-delnp-2005-pct-304.pdf

3356-delnp-2005-pct-409.pdf

3356-delnp-2005-pct-416.pdf


Patent Number 239826
Indian Patent Application Number 3356/DELNP/2005
PG Journal Number 15/2010
Publication Date 09-Apr-2010
Grant Date 05-Apr-2010
Date of Filing 28-Jul-2005
Name of Patentee SASOL TECHNOLOGY (PTY) LTD
Applicant Address 1 STURDEE AVENUE, ROSEBANK, 2196 JOHANNESBURG, SOUTH AFRICA
Inventors:
# Inventor's Name Inventor's Address
1 BOLDER, FRANCISCUS, HERMANUS, ANTONIUS 25 LEIPOLDT STREET, 1947 SASOLBURG, SOUTH AFRICA
PCT International Classification Number B01J 23/28
PCT International Application Number PCT/ZA2004/000007
PCT International Filing date 2004-01-22
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 2003/0585 2003-01-22 Zimbabwe